"Ho hlakile" ho bolela'ng?
Phoofolo ha e jare phetoho ea phetoho. E ke ke ea hlahisa lefu lena mme e ke ke ya e fetisa.
Ntja Centronuclear Myopathy In Border Collie (CNM-BC)
Centronuclear Myopathy (CNM) is a genetic disorder affecting Border Collies, characterized by muscle weakness and exercise intolerance. A DNA test for CNM is essential for responsible breeding, helping to identify carriers and reduce the risk of this debilitating condition. This simple yet effective test enables dog owners and breeders to make informed decisions, ensuring healthier puppies. By understanding the genetic predisposition to CNM, owners can provide better care and management for affected dogs. Regular screening through DNA testing not only promotes the health of individual dogs but also contributes to the overall well-being of the Border Collie breed. Invest in a CNM DNA test today to safeguard your canine companion’s future.
Kgutsufatso : CNM-BC
Phetoho e hlahlobiloeng : DNM2 c.1393C>T
Lefa : Autosomal Recessive
Kgutsufatso
CNM-BC
Khafetsa e shebiloeng
Bohloko ba bongaka
Sehlopha sa bongaka
Mafu a Mesifa
Phetoho e hlahlobiloeng
DNM2 c.1393C>T
p.(R465W)
p.(R465W)
Mokhoa oa lefa
Autosomal Recessive
Kakaretso ea teko:
Centronuclear Myopathy (CNM) is a genetic disorder affecting Border Collies, characterized by muscle weakness and exercise intolerance. A DNA test can identify carriers and affected dogs, enabling breeders to make informed decisions to reduce the prevalence of this condition. Early detection through genetic testing can help owners manage symptoms and improve the quality of life for affected pets. Responsible breeding practices based on test results play a crucial role in preserving the health of the breed. Overall, DNA testing for CNM enhances breed welfare and promotes healthier generations of Border Collies.
E fumaneha ho tsoa paketeng: Basic
Teko ena ea DNA e kenyelelitsoe ho qala ka pakete ea rona Basic - hape ke karolo ea lipakete Basic, Standard, Advanced, Complete.
Sheba Liphutheloana tsa Tlhahlobo ea DNA →Khetha sephutheloana se lumellanang hantle le leano la hau la ho ikatisa kapa bophelo bo botle ba liphoofolo tsa hau.
Overview of Centronuclear Myopathy (CNM) in Border Collies
Centronuclear Myopathy (CNM) is a hereditary muscle disorder found in Border Collies. Characterized by weakness and muscle atrophy, this genetic condition significantly affects the dog's motor capabilities and overall quality of life. CNM results from mutations in specific genes leading to improper muscle fiber development and function.
Matšoao a Bongaka le Matšoao
Dogs affected by CNM typically exhibit clinical signs from a young age. Common symptoms include muscle weakness, reduced physical activity, exercise intolerance, abnormal gait, and muscle wasting. Severely affected dogs may have difficulty standing or walking, potentially impacting their ability to perform routine daily activities.
Genetic Basis of Centronuclear Myopathy
CNM in Border Collies is inherited in an autosomal recessive manner. This means a dog must inherit two copies of the mutated gene—one from each parent—to exhibit symptoms. Dogs carrying only one copy of the mutation (carriers) do not typically show signs but can pass the mutation onto offspring.
Importance of DNA Testing for CNM
DNA testing is essential for identifying the CNM mutation in Border Collies. Early identification of affected and carrier dogs helps breeders make informed decisions, preventing the spread of the condition. DNA testing enables responsible breeding practices, assisting in reducing and eventually eliminating the occurrence of this debilitating condition.
Interpretation of DNA Test Results
The DNA test clearly distinguishes three genetic statuses:
Recommendations for Breeders and Owners
Breeders are advised to conduct CNM DNA testing in breeding dogs before mating. Clear mating strategies should be selected to avoid producing affected puppies. Owners of Border Collies should consult veterinarians and genetic specialists for guidance on managing dogs diagnosed with CNM, ensuring the best possible quality of life.
Mefuta e tsebahalang bakeng sa tlhahlobo : Centronuclear Myopathy In Border Collie (CNM-BC)
- Bearded Collie
- Border Collie
- Farm Collie
- Old Farm Collie
- Rough Collie
- Scottish Collie
- Scottish Rough Collie
- Scottish Smooth Collie
- Smooth Collie
🧬 Interpretation of genotypes CNM-BC
Genotype
Boemo
🟡 N/N
E seng mojari - Ha ho Kotsi
🟡 N/CNM-BC
Mojari - Ha ho Kotsi
❌ CNM-BC/CNM-BC
E angoa - E Kotsing
FAQ: ho utloisisa tlhaloso
Na "Mojari" o tebile?
Che. Ka kakaretso phoofolo ena e phetse hantle empa e ka fetisetsa phetoho eo ho eona bana.
Ho thoe'ng haeba phoofolo e "Ameha"?
E na le likopi tse peli tse fetotsoeng. Matšoao a kliniki a lebelletsoe ho latela lefu lena. Ha ea lokela ho hōlisoa.
Hobaneng ho na le phapang lipakeng tsa monna / mosali?
Mafu a mang a amahanngoa le thobalano, kahoo polelo ea bona e fapana ho latela thobalano ea phoofolo.
Bolela Leloko
N/N (e-seng-mojari)
N/CNM-BC (Mojari)
CNM-BC/CNM-BC (Ametsoe)
DNA Test FAQ
Teko ee ea DNA e sibolla eng?
This DNA test detects the mutation associated with Centronuclear Myopathy In Border Collie (CNM) in order to identify clear, carrier, or at-risk animals.
Ke hobane'ng ha u lokela ho leka phoofolo e tsoalang?
Teko ea DNA e thusa bahlahisi ho rera ho nyalana ho sireletsehileng le ho fokotsa kotsi ea ho fetisetsa phetoho ho bana.
Mokhoa oa lefa oa teko ee ke ofe?
Mokhoa oa lefa o tlalehiloeng bakeng sa tlhahlobo ena ke Autosomal Recessive.
Ke phetoho efe e hlahlobiloeng tekong ee?
This test analyses the mutation DNM2 c.1393C>T.
Na phoofolo e jarang e hlile e amehile?
Eseng hakaalo. Tlhaloso e itšetlehile ka mokhoa oa lefa le genotype e hlahisoang.
Litšupiso
Böhm Johann, Barthélémy Inès, Landwerlin Charlène, BlanchardGutton Nicolas, Relaix Frédéric, Blot Stéphane, Laporte Jocelyn, Tiret Laurent. A dog model for centronuclear myopathy carrying the most common DNM2 mutation. Dis Model Mech. 2022 Apr 1;15(4):dmm049219. doi: 10.1242/dmm.049219. Epub 2022 Apr 14.